CRA II - Sponsor dedicated - Home Based Paris Area
Clinical Careers Page(5 days ago)
About this role
The CRA II at Syneos Health is responsible for site management activities related to clinical trials, ensuring compliance with regulatory standards and study protocols. The role includes site qualification, initiation, monitoring, and close-out activities, either remotely or on-site, to facilitate clinical research processes in accordance with Good Clinical Practice guidelines.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Site Management
- Source Document Review
- Data Entry
- Investigator Liaison
- Clinical Data Management
- Regulatory Compliance
- Pharmacovigilance
About Clinical Careers Page
syneoshealth.comSyneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.
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